-
3
-
-
84867744264
-
Evolution of the cancer genome
-
L.R. Yates, and P.J. Campbell Evolution of the cancer genome Nat Rev Genet 13 2014 795 806
-
(2014)
Nat Rev Genet
, vol.13
, pp. 795-806
-
-
Yates, L.R.1
Campbell, P.J.2
-
4
-
-
84864402732
-
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly
-
J.H. Lee, M. Huynh, J.L. Silhavy, S. Kim, T. Dixon-Salazar, A. Heiberg, and et al. De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly Nat Genet 44 2012 941 945
-
(2012)
Nat Genet
, vol.44
, pp. 941-945
-
-
Lee, J.H.1
Huynh, M.2
Silhavy, J.L.3
Kim, S.4
Dixon-Salazar, T.5
Heiberg, A.6
-
5
-
-
84859646140
-
Somatic activation of AKT3 causes hemispheric developmental brain malformations
-
A. Poduri, G.D. Evrony, X. Cai, P.C. Elhosary, R. Beroukhim, M.K. Lehtinen, and et al. Somatic activation of AKT3 causes hemispheric developmental brain malformations Neuron 74 2012 41 48
-
(2012)
Neuron
, vol.74
, pp. 41-48
-
-
Poduri, A.1
Evrony, G.D.2
Cai, X.3
Elhosary, P.C.4
Beroukhim, R.5
Lehtinen, M.K.6
-
6
-
-
84907313347
-
Somatic mutations in cerebral cortical malformations
-
S.S. Jamuar, A.T. Lam, M. Kircher, A.M. D'Gama, J. Wang, B.J. Barry, and et al. Somatic mutations in cerebral cortical malformations N Engl J Med 371 2014 733 743
-
(2014)
N Engl J Med
, vol.371
, pp. 733-743
-
-
Jamuar, S.S.1
Lam, A.T.2
Kircher, M.3
D'Gama, A.M.4
Wang, J.5
Barry, B.J.6
-
7
-
-
84906850648
-
The diverse genetic landscape of neurodevelopmental disorders
-
W.F. Hu, M.H. Chahrour, and C.A. Walsh The diverse genetic landscape of neurodevelopmental disorders Annu Rev Genomics Hum Genet 15 2014 195 213
-
(2014)
Annu Rev Genomics Hum Genet
, vol.15
, pp. 195-213
-
-
Hu, W.F.1
Chahrour, M.H.2
Walsh, C.A.3
-
8
-
-
76549128519
-
Evolution in health and medicine Sackler colloquium: Somatic evolutionary genomics: Mutations during development cause highly variable genetic mosaicism with risk of cancer and neurodegeneration
-
S.A. Frank Evolution in health and medicine Sackler colloquium: somatic evolutionary genomics: mutations during development cause highly variable genetic mosaicism with risk of cancer and neurodegeneration Proc Natl Acad Sci U S A 107 Suppl 1 2010 1725 1730
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 1725-1730
-
-
Frank, S.A.1
-
9
-
-
1942467937
-
Somatic mutation: A cause of sporadic neurodegenerative diseases?
-
R. Pamphlett Somatic mutation: a cause of sporadic neurodegenerative diseases? Med Hypotheses 62 2004 679 682
-
(2004)
Med Hypotheses
, vol.62
, pp. 679-682
-
-
Pamphlett, R.1
-
10
-
-
84879756120
-
Somatic mutation, genomic variation, and neurological disease
-
A. Poduri, G.D. Evrony, X. Cai, and C.A. Walsh Somatic mutation, genomic variation, and neurological disease Science 341 2013 1237758
-
(2013)
Science
, vol.341
, pp. 1237758
-
-
Poduri, A.1
Evrony, G.D.2
Cai, X.3
Walsh, C.A.4
-
11
-
-
84879603430
-
Somatic alpha-synuclein mutations in Parkinson's disease: Hypothesis and preliminary data
-
C. Proukakis, H. Houlden, and A.H. Schapira Somatic alpha-synuclein mutations in Parkinson's disease: hypothesis and preliminary data Mov Disord 28 2013 705 712
-
(2013)
Mov Disord
, vol.28
, pp. 705-712
-
-
Proukakis, C.1
Houlden, H.2
Schapira, A.H.3
-
12
-
-
17844395196
-
Aneuploid neurons are functionally active and integrated into brain circuitry
-
M.A. Kingsbury, B. Friedman, M.J. McConnell, S.K. Rehen, A.H. Yang, D. Kaushal, and et al. Aneuploid neurons are functionally active and integrated into brain circuitry Proc Natl Acad Sci U S A 102 2005 6143 6147
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 6143-6147
-
-
Kingsbury, M.A.1
Friedman, B.2
McConnell, M.J.3
Rehen, S.K.4
Yang, A.H.5
Kaushal, D.6
-
13
-
-
33745593721
-
Generation of neuronal variability and complexity
-
A.R. Muotri, and F.H. Gage Generation of neuronal variability and complexity Nature 441 2006 1087 1093
-
(2006)
Nature
, vol.441
, pp. 1087-1093
-
-
Muotri, A.R.1
Gage, F.H.2
-
14
-
-
84922584195
-
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain
-
X. Cai, G.D. Evrony, H.S. Lehmann, P.C. Elhosary, B.K. Mehta, A. Poduri, and et al. Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain Cell Rep 8 2014 1280 1289
-
(2014)
Cell Rep
, vol.8
, pp. 1280-1289
-
-
Cai, X.1
Evrony, G.D.2
Lehmann, H.S.3
Elhosary, P.C.4
Mehta, B.K.5
Poduri, A.6
-
16
-
-
84907737648
-
Genome sequencing of normal cells reveals developmental lineages and mutational processes
-
S. Behjati, M. Huch, R. van Boxtel, W. Karthaus, D.C. Wedge, A.U. Tamuri, and et al. Genome sequencing of normal cells reveals developmental lineages and mutational processes Nature 513 2014 422 425
-
(2014)
Nature
, vol.513
, pp. 422-425
-
-
Behjati, S.1
Huch, M.2
Van Boxtel, R.3
Karthaus, W.4
Wedge, D.C.5
Tamuri, A.U.6
-
17
-
-
64549116740
-
Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain
-
F.A. Azevedo, L.R. Carvalho, L.T. Grinberg, J.M. Farfel, R.E. Ferretti, R.E. Leite, and et al. Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain J Comp Neurol 513 2009 532 541
-
(2009)
J Comp Neurol
, vol.513
, pp. 532-541
-
-
Azevedo, F.A.1
Carvalho, L.R.2
Grinberg, L.T.3
Farfel, J.M.4
Ferretti, R.E.5
Leite, R.E.6
-
18
-
-
3042856300
-
Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease
-
J.A. Beck, M. Poulter, T.A. Campbell, J.B. Uphill, G. Adamson, J.F. Geddes, and et al. Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease Hum Mol Genet 13 2004 1219 1224
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1219-1224
-
-
Beck, J.A.1
Poulter, M.2
Campbell, T.A.3
Uphill, J.B.4
Adamson, G.5
Geddes, J.F.6
-
19
-
-
0033358671
-
Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum
-
D. Campion, C. Dumanchin, D. Hannequin, B. Dubois, S. Belliard, M. Puel, and et al. Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum Am J Hum Genet 65 1999 664 670
-
(1999)
Am J Hum Genet
, vol.65
, pp. 664-670
-
-
Campion, D.1
Dumanchin, C.2
Hannequin, D.3
Dubois, B.4
Belliard, S.5
Puel, M.6
-
21
-
-
72149125838
-
The transcellular spread of cytosolic amyloids, prions, and prionoids
-
A. Aguzzi, and L. Rajendran The transcellular spread of cytosolic amyloids, prions, and prionoids Neuron 64 2009 783 790
-
(2009)
Neuron
, vol.64
, pp. 783-790
-
-
Aguzzi, A.1
Rajendran, L.2
-
22
-
-
0034657130
-
Evidence for seeding of beta-amyloid by intracerebral infusion of Alzheimer brain extracts in beta-amyloid precursor protein-transgenic mice
-
M.D. Kane, W.J. Lipinski, M.J. Callahan, F. Bian, R.A. Durham, R.D. Schwarz, and et al. Evidence for seeding of beta-amyloid by intracerebral infusion of Alzheimer brain extracts in beta-amyloid precursor protein-transgenic mice J Neurosci 20 2000 3606 3611
-
(2000)
J Neurosci
, vol.20
, pp. 3606-3611
-
-
Kane, M.D.1
Lipinski, W.J.2
Callahan, M.J.3
Bian, F.4
Durham, R.A.5
Schwarz, R.D.6
-
23
-
-
78149392229
-
Peripherally applied Abeta-containing inoculates induce cerebral beta-amyloidosis
-
Y.S. Eisele, U. Obermuller, G. Heilbronner, F. Baumann, S.A. Kaeser, H. Wolburg, and et al. Peripherally applied Abeta-containing inoculates induce cerebral beta-amyloidosis Science 330 2010 980 982
-
(2010)
Science
, vol.330
, pp. 980-982
-
-
Eisele, Y.S.1
Obermuller, U.2
Heilbronner, G.3
Baumann, F.4
Kaeser, S.A.5
Wolburg, H.6
-
24
-
-
67650077008
-
Transmission and spreading of tauopathy in transgenic mouse brain
-
F. Clavaguera, T. Bolmont, R.A. Crowther, D. Abramowski, S. Frank, A. Probst, and et al. Transmission and spreading of tauopathy in transgenic mouse brain Nat Cell Biol 11 2009 909 913
-
(2009)
Nat Cell Biol
, vol.11
, pp. 909-913
-
-
Clavaguera, F.1
Bolmont, T.2
Crowther, R.A.3
Abramowski, D.4
Frank, S.5
Probst, A.6
-
25
-
-
84857275902
-
Propagation of tau pathology in a model of early Alzheimer's disease
-
A. de Calignon, M. Polydoro, M. Suarez-Calvet, C. William, D.H. Adamowicz, K.J. Kopeikina, and et al. Propagation of tau pathology in a model of early Alzheimer's disease Neuron 73 2012 685 697
-
(2012)
Neuron
, vol.73
, pp. 685-697
-
-
De Calignon, A.1
Polydoro, M.2
Suarez-Calvet, M.3
William, C.4
Adamowicz, D.H.5
Kopeikina, K.J.6
-
26
-
-
77954380684
-
Comparison of Sanger sequencing, pyrosequencing, and melting curve analysis for the detection of KRAS mutations: Diagnostic and clinical implications
-
A.C. Tsiatis, A. Norris-Kirby, R.G. Rich, M.J. Hafez, C.D. Gocke, J.R. Eshleman, and et al. Comparison of Sanger sequencing, pyrosequencing, and melting curve analysis for the detection of KRAS mutations: diagnostic and clinical implications J Mol Diagn 12 2010 425 432
-
(2010)
J Mol Diagn
, vol.12
, pp. 425-432
-
-
Tsiatis, A.C.1
Norris-Kirby, A.2
Rich, R.G.3
Hafez, M.J.4
Gocke, C.D.5
Eshleman, J.R.6
-
27
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
H. Li, and R. Durbin Fast and accurate short read alignment with Burrows-Wheeler transform Bioinformatics 25 2009 1754 1760
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
28
-
-
68549104404
-
The sequence alignment/map format and SAMtools
-
H. Li, B. Handsaker, A. Wysoker, T. Fennell, J. Ruan, N. Homer, and et al. The sequence alignment/map format and SAMtools Bioinformatics 25 2009 2078 2079
-
(2009)
Bioinformatics
, vol.25
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
Homer, N.6
-
29
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
A. McKenna, M. Hanna, E. Banks, A. Sivachenko, K. Cibulskis, A. Kernytsky, and et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data Genome Res 20 2010 1297 1303
-
(2010)
Genome Res
, vol.20
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
-
30
-
-
84863229597
-
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
-
D.C. Koboldt, Q. Zhang, D.E. Larson, D. Shen, M.D. McLellan, L. Lin, and et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing Genome Res 22 2012 568 576
-
(2012)
Genome Res
, vol.22
, pp. 568-576
-
-
Koboldt, D.C.1
Zhang, Q.2
Larson, D.E.3
Shen, D.4
McLellan, M.D.5
Lin, L.6
-
31
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
K. Wang, M. Li, and H. Hakonarson ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data Nucleic Acids Res 38 2010 e164
-
(2010)
Nucleic Acids Res
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
32
-
-
84884521244
-
Accurately identifying low-allelic fraction variants in single samples with next-generation sequencing: Applications in tumor subclone resolution
-
L.F. Stead, K.M. Sutton, G.R. Taylor, P. Quirke, and P. Rabbitts Accurately identifying low-allelic fraction variants in single samples with next-generation sequencing: applications in tumor subclone resolution Hum Mutat 34 2013 1432 1438
-
(2013)
Hum Mutat
, vol.34
, pp. 1432-1438
-
-
Stead, L.F.1
Sutton, K.M.2
Taylor, G.R.3
Quirke, P.4
Rabbitts, P.5
-
33
-
-
79954553212
-
Improving SNP discovery by base alignment quality
-
H. Li Improving SNP discovery by base alignment quality Bioinformatics 27 2011 1157 1158
-
(2011)
Bioinformatics
, vol.27
, pp. 1157-1158
-
-
Li, H.1
-
34
-
-
84884647935
-
The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-epsilon4 carriers
-
B.A. Benitez, C.M. Karch, Y. Cai, S.C. Jin, B. Cooper, D. Carrell, and et al. The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-epsilon4 carriers PLoS Genet 9 2013 e1003685
-
(2013)
PLoS Genet
, vol.9
, pp. e1003685
-
-
Benitez, B.A.1
Karch, C.M.2
Cai, Y.3
Jin, S.C.4
Cooper, B.5
Carrell, D.6
-
35
-
-
84856541277
-
Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families
-
C. Cruchaga, G. Haller, S. Chakraverty, K. Mayo, F.L. Vallania, R.D. Mitra, and et al. Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families PLoS One 7 2012 e31039
-
(2012)
PLoS One
, vol.7
, pp. e31039
-
-
Cruchaga, C.1
Haller, G.2
Chakraverty, S.3
Mayo, K.4
Vallania, F.L.5
Mitra, R.D.6
-
36
-
-
0033545946
-
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
-
I. D'Souza, P. Poorkaj, M. Hong, D. Nochlin, V.M. Lee, T.D. Bird, and et al. Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements Proc Natl Acad Sci U S A 96 1999 5598 5603
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 5598-5603
-
-
D'Souza, I.1
Poorkaj, P.2
Hong, M.3
Nochlin, D.4
Lee, V.M.5
Bird, T.D.6
-
37
-
-
84876592083
-
A genomic view of mosaicism and human disease
-
L.G. Biesecker, and N.B. Spinner A genomic view of mosaicism and human disease Nat Rev Genet 14 2013 307 320
-
(2013)
Nat Rev Genet
, vol.14
, pp. 307-320
-
-
Biesecker, L.G.1
Spinner, N.B.2
-
38
-
-
77951702768
-
Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis
-
L.K. Conlin, B.D. Thiel, C.G. Bonnemann, L. Medne, L.M. Ernst, E.H. Zackai, and et al. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis Hum Mol Genet 19 2010 1263 1275
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1263-1275
-
-
Conlin, L.K.1
Thiel, B.D.2
Bonnemann, C.G.3
Medne, L.4
Ernst, L.M.5
Zackai, E.H.6
-
39
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
I.A. Adzhubei, S. Schmidt, L. Peshkin, V.E. Ramensky, A. Gerasimova, P. Bork, and et al. A method and server for predicting damaging missense mutations Nat Methods 7 2010 248 249
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
-
40
-
-
56349119351
-
Linking Abeta and tau in late-onset Alzheimer's disease: A dual pathway hypothesis
-
S.A. Small, and K. Duff Linking Abeta and tau in late-onset Alzheimer's disease: a dual pathway hypothesis Neuron 60 2008 534 542
-
(2008)
Neuron
, vol.60
, pp. 534-542
-
-
Small, S.A.1
Duff, K.2
-
41
-
-
0344152227
-
Identification of new presenilin gene mutations in early-onset familial Alzheimer disease
-
A. Tedde, B. Nacmias, M. Ciantelli, P. Forleo, E. Cellini, S. Bagnoli, and et al. Identification of new presenilin gene mutations in early-onset familial Alzheimer disease Arch Neurol 60 2003 1541 1544
-
(2003)
Arch Neurol
, vol.60
, pp. 1541-1544
-
-
Tedde, A.1
Nacmias, B.2
Ciantelli, M.3
Forleo, P.4
Cellini, E.5
Bagnoli, S.6
-
42
-
-
33947145598
-
Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease
-
C. Tomaino, L. Bernardi, M. Anfossi, A. Costanzo, F. Ferrise, M. Gallo, and et al. Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease J Neurol 254 2007 391 393
-
(2007)
J Neurol
, vol.254
, pp. 391-393
-
-
Tomaino, C.1
Bernardi, L.2
Anfossi, M.3
Costanzo, A.4
Ferrise, F.5
Gallo, M.6
-
43
-
-
84911430470
-
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease
-
C. Sassi, R. Guerreiro, R. Gibbs, J. Ding, M.K. Lupton, C. Troakes, and et al. Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's disease Neurobiol Aging 35 2014 2881.e1 2881.e6
-
(2014)
Neurobiol Aging
, vol.35
, pp. 2881e1-2881e6
-
-
Sassi, C.1
Guerreiro, R.2
Gibbs, R.3
Ding, J.4
Lupton, M.K.5
Troakes, C.6
-
44
-
-
84868030363
-
Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort
-
S.C. Jin, P. Pastor, B. Cooper, S. Cervantes, B.A. Benitez, C. Razquin, and et al. Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort Alzheimers Res Ther 4 2012 34
-
(2012)
Alzheimers Res Ther
, vol.4
, pp. 34
-
-
Jin, S.C.1
Pastor, P.2
Cooper, B.3
Cervantes, S.4
Benitez, B.A.5
Razquin, C.6
-
45
-
-
84903818205
-
Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease
-
C. Sassi, R. Guerreiro, R. Gibbs, J. Ding, M.K. Lupton, C. Troakes, and et al. Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease Neurobiol Aging 35 2014 2422.e13 2422.e16
-
(2014)
Neurobiol Aging
, vol.35
, pp. 2422e13-2422e16
-
-
Sassi, C.1
Guerreiro, R.2
Gibbs, R.3
Ding, J.4
Lupton, M.K.5
Troakes, C.6
-
46
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
R. Sherrington, E.I. Rogaev, Y. Liang, E.A. Rogaeva, G. Levesque, M. Ikeda, and et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease Nature 375 1995 754 760
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
-
47
-
-
0035026704
-
Predicting deleterious amino acid substitutions
-
P.C. Ng, and S. Henikoff Predicting deleterious amino acid substitutions Genome Res 11 2001 863 874
-
(2001)
Genome Res
, vol.11
, pp. 863-874
-
-
Ng, P.C.1
Henikoff, S.2
-
48
-
-
0028812820
-
Mutations of the presenilin i gene in families with early-onset Alzheimer's disease
-
D. Campion, J.M. Flaman, A. Brice, D. Hannequin, B. Dubois, C. Martin, and et al. Mutations of the presenilin I gene in families with early-onset Alzheimer's disease Hum Mol Genet 4 1995 2373 2377
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2373-2377
-
-
Campion, D.1
Flaman, J.M.2
Brice, A.3
Hannequin, D.4
Dubois, B.5
Martin, C.6
-
49
-
-
34848922135
-
APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage
-
A. Rovelet-Lecrux, T. Frebourg, H. Tuominen, K. Majamaa, D. Campion, and A.M. Remes APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage J Neurol Neurosurg Psychiatry 78 2007 1158 1159
-
(2007)
J Neurol Neurosurg Psychiatry
, vol.78
, pp. 1158-1159
-
-
Rovelet-Lecrux, A.1
Frebourg, T.2
Tuominen, H.3
Majamaa, K.4
Campion, D.5
Remes, A.M.6
-
50
-
-
0025863618
-
Neuropathological stageing of Alzheimer-related changes
-
H. Braak, and E. Braak Neuropathological stageing of Alzheimer-related changes Acta Neuropathol 82 1991 239 259
-
(1991)
Acta Neuropathol
, vol.82
, pp. 239-259
-
-
Braak, H.1
Braak, E.2
|